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The Efficacy of Hydrolyzed Guar Gum ( PHGG) in the Treatment of Patients With Irritable Bowel Syndrome (IBS)

The Efficacy of Hydrolyzed Guar Gum ( PHGG) in the Treatment of Patients With Irritable Bowel Syndrome- a Double Blind, Placebo - Controlled, Randomized Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01779765
Enrollment
130
Registered
2013-01-30
Start date
2013-01-31
Completion date
2014-06-30
Last updated
2014-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

IBS

Keywords

IBS, Diarrhea, Constipation, Fibers

Brief summary

This study objective is to assess the short and long term effects of partially hydrolyzed guar gum (PHGG) administration on clinical symptoms of IBS and quality of life of these patients.

Interventions

DIETARY_SUPPLEMENTPHGG
DIETARY_SUPPLEMENTMaltodextrin

Sponsors

Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Fulfillment of the Rome III criteria for IBS. * Aged 20-68 years at the time of screening. * Provision of written informed consent. * Commitment of availability throughout the 6 months study period.

Exclusion criteria

* Major abdominal surgery in the past. * The presence of any active (organic)GI disease. * Past or present major medical or psychiatric illness. * Any concomitant disease. * Alarming symptoms (rectal bleeding, weight loss, etc.) * Pregnancy. * Family history of colorectal carcinoma or inflammatory bowel disease (IBD). * Abnormal laboratory studies (blood biochemistry , liver enzymes,complete blood count), abnormal thyroid function. * Non-adjusted diet in the case of lactose or gluten intolerance. * Recent travel to regions with endemic parasitic diseases.

Design outcomes

Primary

MeasureTime frameDescription
Improvement in IBS score.2 yearsIBS scoring - Francis severity IBS score.

Secondary

MeasureTime frameDescription
Quality questionnaire2 yearsQuality of life - by the IBS - quality of life questionnaire - Drossman Patrick.

Countries

Israel

Contacts

Primary ContactNachum Vaisman, MD
vaisman@tasmc.health.gov.il972-3-6974807

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026